Canonical Allele Identifier: CA913077125
Gene: ACADM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75740048_75740051del , CM000663.2:g.75740048_75740051del GRCh38
NC_000001.10:g.76205733_76205736del , CM000663.1:g.76205733_76205736del GRCh37
NC_000001.9:g.75978321_75978324del NCBI36
NG_007045.2:g.20691_20694del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370841.9:c.537_540del MANE Select ENSP00000359878.5:p.Gly180MetfsTer12
ENST00000473018.3:n.2661_2664del
ENST00000541113.6:c.537_540del ENSP00000442324.2:p.Gly180MetfsTer12
ENST00000679509.1:n.1499_1502del
ENST00000679530.1:c.*305_*308del ENSP00000506454.1:n.*305_*308del
ENST00000679615.1:n.2661_2664del
ENST00000679687.1:c.99_102del ENSP00000506598.1:p.Gly34MetfsTer12
ENST00000679704.1:c.*303_*306del ENSP00000505117.1:n.*303_*306del
ENST00000679709.1:c.*500_*503del ENSP00000506623.1:n.*500_*503del
ENST00000679804.1:n.276_279del
ENST00000679976.1:c.*121_*124del ENSP00000505565.1:n.*121_*124del
ENST00000680166.1:n.3826_3829del
ENST00000680517.1:c.*34_*37del ENSP00000505803.1:n.*34_*37del
ENST00000680582.1:n.1499_1502del
ENST00000680613.1:c.537_540del ENSP00000506114.1:p.Gly180MetfsTer12
ENST00000680662.1:c.*451_*454del ENSP00000505080.1:n.*451_*454del
ENST00000680691.1:c.*200_*203del ENSP00000506487.1:n.*200_*203del
ENST00000680694.1:c.*125_*128del ENSP00000505658.1:n.*125_*128del
ENST00000680743.1:c.*204_*207del ENSP00000505073.1:n.*204_*207del
ENST00000680749.1:c.537_540del ENSP00000505122.1:p.Gly180MetfsTer12
ENST00000680798.1:c.*121_*124del ENSP00000505670.1:n.*121_*124del
ENST00000680805.1:c.537_540del ENSP00000505447.1:p.Gly180MetfsTer12
ENST00000680844.1:c.*321_*324del ENSP00000506541.1:n.*321_*324del
ENST00000680948.1:c.*404_*407del ENSP00000505441.1:n.*404_*407del
ENST00000680964.1:c.537_540del ENSP00000505961.1:p.Gly180MetfsTer12
ENST00000681037.1:c.537_540del ENSP00000506025.1:p.Gly180MetfsTer12
ENST00000681063.1:c.537_540del ENSP00000506616.1:p.Gly180MetfsTer12
ENST00000681209.1:c.*301_*304del ENSP00000505877.1:n.*301_*304del
ENST00000681278.1:n.894_897del
ENST00000681289.1:n.894_897del
ENST00000681361.1:c.*204_*207del ENSP00000506679.1:n.*204_*207del
ENST00000681430.1:c.537_540del ENSP00000506301.1:p.Gly180MetfsTer12
ENST00000681446.1:c.*119_*122del ENSP00000506244.1:n.*119_*122del
ENST00000681450.1:c.*208_*211del ENSP00000505660.1:n.*208_*211del
ENST00000681548.1:c.*123_*126del ENSP00000505275.1:n.*123_*126del
ENST00000681616.1:c.*305_*308del ENSP00000505111.1:n.*305_*308del
ENST00000681621.1:c.*121_*124del ENSP00000505770.1:n.*121_*124del
ENST00000681680.1:n.2661_2664del
ENST00000681720.1:c.*55-5758_*55-5755del ENSP00000505438.1:n.*55-5758_*55-5755del
ENST00000681730.1:n.759_762del
ENST00000681790.1:c.279_282del ENSP00000505130.1:p.Gly94MetfsTer12
ENST00000681837.1:n.1153_1156del
ENST00000681913.1:n.2661_2664del
ENST00000681916.1:c.*305_*308del ENSP00000506477.1:n.*305_*308del
ENST00000681930.1:n.2661_2664del
ENST00000370834.9:c.636_639del ENSP00000359871.5:p.Gly213MetfsTer12
ENST00000370841.8:c.537_540del ENSP00000359878.4:p.Gly180MetfsTer12
ENST00000420607.6:c.549_552del ENSP00000409612.2:p.Gly184MetfsTer12
ENST00000525808.5:c.*123_*126del ENSP00000434823.1:n.*123_*126del
ENST00000526129.5:c.*321_*324del ENSP00000434092.1:n.*321_*324del
ENST00000526196.5:c.*305_*308del ENSP00000431953.1:n.*305_*308del
ENST00000526930.1:n.310_313del
ENST00000529059.5:n.446_449del
ENST00000530953.6:c.*34_*37del ENSP00000431372.1:n.*34_*37del
ENST00000532509.5:c.*301_*304del ENSP00000432522.1:n.*301_*304del
ENST00000534334.5:c.*121_*124del ENSP00000435584.1:n.*121_*124del
ENST00000541113.5:c.429_432del ENSP00000442324.1:p.Gly144MetfsTer12
NM_000016.5:c.537_540del NP_000007.1:p.Gly180MetfsTer12
NM_001127328.2:c.549_552del NP_001120800.1:p.Gly184MetfsTer12
NM_001286042.1:c.429_432del NP_001272971.1:p.Gly144MetfsTer12
NM_001286043.1:c.636_639del NP_001272972.1:p.Gly213MetfsTer12
NM_001286044.1:c.-31_-28del NP_001272973.1:n.-31_-28del
NM_000016.6:c.537_540del MANE Select NP_000007.1:p.Gly180MetfsTer12
NM_001127328.3:c.549_552del NP_001120800.1:p.Gly184MetfsTer12
NM_001286042.2:c.429_432del NP_001272971.1:p.Gly144MetfsTer12
NM_001286043.2:c.636_639del NP_001272972.1:p.Gly213MetfsTer12
NM_001286044.2:c.-31_-28del NP_001272973.1:n.-31_-28del